Acetate supplementation restores cognitive deficits caused by ARID1A haploinsufficiency in excitatory neurons

Mutations in AT‐rich interactive domain‐containing protein 1A (ARID1A) cause Coffin‐Siris syndrome (CSS), a rare genetic disorder that results in mild to severe intellectual disabilities. However, the biological role of ARID1A in the brain remains unclear. In this study, we report that the haploinsu...

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Detalles Bibliográficos
Autores principales: Liu, Pei‐Pei, Dai, Shang‐Kun, Mi, Ting‐Wei, Tang, Gang‐Bin, Wang, Zhuo, Wang, Hui, Du, Hong‐Zhen, Tang, Yi, Teng, Zhao‐Qian, Liu, Chang‐Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728054/
https://www.ncbi.nlm.nih.gov/pubmed/36385502
http://dx.doi.org/10.15252/emmm.202215795

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728054/
https://www.ncbi.nlm.nih.gov/pubmed/36385502
http://dx.doi.org/10.15252/emmm.202215795

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